Authors:
HO Fearnhead, J Rodriguez, EE Govek, W Guo, R Kobayashi, G Hannon, YA Lazebnik
Journal name: 
Proc Natl Acad Sci U S A
Citation info: 
95(23):13664-13669
Abstract: 
Understanding how oncogenic transformation sensitizes cells to apoptosis may provide a strategy to kill tumor cells selectively. We previously developed a cell-free system that recapitulates oncogene dependent apoptosis as reflected by activation of caspases, the core of the apoptotic machinery. Here, we show that this activation requires a previously identified apoptosis-promoting complex consisting of caspase-9, APAF-1, and cytochrome c. As predicted by the in vitro system, preventing caspase-9 activation blocked drug-induced apoptosis in cells sensitized by E1A, an adenoviral oncogene. Oncogenes, such as E1A, appear to facilitate caspase-9 activation by several mechanisms, including the control of cytochrome c release from the mitochondria.
DOI: 
http://doi.org/10.1073/pnas.95.23.13664
Research group: 
Hannon Group
E-pub date: 
31 Oct 1998
Users with this publication listed: 
Greg Hannon